Elevated expression of the proto-oncogene c-kit in patients with mastocytosis

被引:26
作者
Nagata, H [1 ]
Worobec, AS [1 ]
Semere, T [1 ]
Metcalfe, DD [1 ]
机构
[1] NIAID, Lab Allerg Dis, NIH, Bethesda, MD 20892 USA
关键词
c-kit; mastocytosis; stem cell factor; mast cells;
D O I
10.1038/sj.leu.2400906
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The stem cell factor (SCF)c-kit receptor interaction plays a critical role in the development and survival of mast cells, Several studies have also associated c-kit receptor mutations with the human diseases, mastocytosis and piebaldism. Overexpression of c-kit has been reported to be associated with myeloproliferative disorders and myelodysplastic syndromes. Using peripheral blood mononuclear cells (PBMCs) from II patients with indolent mastocytosis (category I), mastocytosis with an associated hematologic disorder (category II), or aggressive mastocytosis (category III); a patient with CMML unassociated with mastocytosis, and PBMCs from 13 normal subjects, we examined the level of expression of c-kit mRNA along with other c-kit isoforms to determine if overexpression of the c-kit receptor was associated with mastocytosis. Using quantitative competitive PCR, c-kif mRNA levels on average were found to be statistically elevated in the five patients with mastocytosis with an associated hematologic disorder and in the patient with aggressive mastocytosis as compared with controls, but not elevated in patients with indolent mastocytosis, The relative mRNA expression for the two c-kit isoforms was not significantly different in the mastocytosis patients compared with controls. This demonstration of the overexpression of c-kit mRNA in mastocytosis, and particularly those patients with clinical evidence of myelodysplastic syndrome, adds evidence to support the conclusion that mastocytosis, at least in some patients, is a feature of myelodysplasia; and suggests that determination of c-kit mRNA expression in PBMCs may provide an additional approach to assessing prognosis.
引用
收藏
页码:175 / 181
页数:7
相关论文
共 37 条
[1]  
AGIS H, 1993, J IMMUNOL, V151, P4221
[2]  
ASHMAN LK, 1991, BLOOD, V78, P30
[3]   ESTABLISHMENT OF AN IMMATURE MAST-CELL LINE FROM A PATIENT WITH MAST-CELL LEUKEMIA [J].
BUTTERFIELD, JH ;
WEILER, D ;
DEWALD, G ;
GLEICH, GJ .
LEUKEMIA RESEARCH, 1988, 12 (04) :345-355
[4]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[5]  
CROSIER PS, 1993, BLOOD, V82, P1151
[6]   HUMAN PIEBALD TRAIT RESULTING FROM A DOMINANT NEGATIVE MUTANT ALLELE OF THE C-KIT MEMBRANE-RECEPTOR GENE [J].
FLEISCHMAN, RA .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (06) :1713-1717
[7]   DELETION OF THE C-KIT PROTOONCOGENE IN THE HUMAN DEVELOPMENTAL DEFECT PIEBALD TRAIT [J].
FLEISCHMAN, RA ;
SALTMAN, DL ;
STASTNY, V ;
ZNEIMER, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (23) :10885-10889
[8]   C-KIT-KINASE INDUCES A CASCADE OF PROTEIN TYROSINE PHOSPHORYLATION IN NORMAL HUMAN MELANOCYTES IN RESPONSE TO MAST-CELL GROWTH-FACTOR AND STIMULATES MITOGEN-ACTIVATED PROTEIN-KINASE BUT IS DOWN-REGULATED IN MELANOMAS [J].
FUNASAKA, Y ;
BOULTON, T ;
COBB, M ;
YARDEN, Y ;
FAN, BL ;
LYMAN, SD ;
WILLIAMS, DE ;
ANDERSON, DM ;
ZAKUT, R ;
MISHIMA, Y ;
HALABAN, R .
MOLECULAR BIOLOGY OF THE CELL, 1992, 3 (02) :197-209
[9]   IDENTIFICATION OF MUTATIONS IN THE CODING SEQUENCE OF THE PROTOONCOGENE C-KIT IN A HUMAN MAST-CELL LEUKEMIA-CELL LINE CAUSING LIGAND-INDEPENDENT ACTIVATION OF C-KIT PRODUCT [J].
FURITSU, T ;
TSUJIMURA, T ;
TONO, T ;
IKEDA, H ;
KITAYAMA, H ;
KOSHIMIZU, U ;
SUGAHARA, H ;
BUTTERFIELD, JH ;
ASHMAN, LK ;
KANAYAMA, Y ;
MATSUZAWA, Y ;
KITAMURA, Y ;
KANAKURA, Y .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (04) :1736-1744
[10]  
Gelfand D.H., 1990, PC PRO, P129